Sector News

Otonomy axes staff, hits brakes on R&D

September 14, 2017
Life sciences

Otonomy is hunkering down after a phase 3 wipeout devastated its near-term prospects. The ear disease firm is laying off one-third of its noncommercial staff and hitting pause on its remaining pipeline programs.

San Diego, California-based Otonomy unveiled the cuts and pipeline review two weeks after the failure of Otividex to move the needle in phase 3 forced it to can that candidate. The aftershocks of the blow are being felt well beyond the Otividex program. Otonomy is holding off on starting clinical trials of other candidates until next year at the earliest.

That means the progress of OTO-311 into a phase 2 tinnitus trial and Otiprio into a pivotal study in children with acute otitis media with tympanostomy tubes is on hold. Otonomy will decide on the timing of the study starts as part of a reassessment of its pipeline.

Whatever Otonomy decides, it will move forward with a reduced workforce. The ax is set to fall on one-third of the Otonomy staff who work on tasks other than the commercialization of Otiprio. Otonomy’s total headcount was 139 as of the end of 2016. The biotech’s sales force stood at 40 before a recent reorganization, suggesting the latest cuts could affect about 30 employees.

Otonomy thinks the cuts are necessary if it is to bounce back from the phase 3 setback.

“We moved quickly following the disappointing AVERTS-1 trial results to focus our efforts in order to reduce costs,” Otonomy CEO David Weber, Ph.D., said in a statement. “The changes we are making give us the cash runway we need to build shareholder value by focusing on key assets in our product pipeline which we believe is still the broadest in the otology field.”

Expectations for that pipeline have been beaten down by Otonomy’s failures in the clinic and its struggles to grow sales of Otiprio, which won FDA approval late in 2015. Sales in the most recent quarter came in at $300,000, up from $100,000 a year earlier. The FDA is due to decide whether to also approve Otiprio in acute otitis externa, a bacterial infection also known as swimmer’s ear, by March.

By Nick Paul Taylor

Source: Fierce Biotech

comments closed

Related News

April 20, 2024

CureVac and MD Anderson Cancer Center partner to develop new cancer vaccines

Life sciences

CureVac and the University of Texas’s MD Anderson Cancer Center have announced a co-development and licensing agreement to develop novel messenger ribonucleic acid (mRNA)-based cancer vaccines. The strategic collaboration will focus on the development of differentiated cancer vaccine candidates in selected haematological and solid tumour indications with high unmet medical needs.

April 20, 2024

FUJIFILM plans $1.2 billion investment in major US manufacturing facility

Life sciences

FUJIFILM Corporation is planning to invest $1.2 billion to expand the planned FUJIFILM Diosynth Biotechnologies manufacturing facility in Holly Springs, North Carolina, US. This news follows the organisation’s announcement of a $2 billion investment in the facility in March 2021. This additional financial boost totals the investment to over $3.2 billion, FUJIFILM confirmed.

April 20, 2024

Sanofi cuts staff in Belgium as early-stage research dwindles

Life sciences

Sanofi’s global restructuring and downsizing is now fully underway, with layoffs stretching to the company’s Belgian offices. Belgian newspaper De Tijd reports that 67 employees have been laid off at a site in Ghent and 32 jobs are on the chopping block at Sanofi’s Belgium HQ in Diegem.

How can we help you?

We're easy to reach